Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:66924693-66925093 | Common:3; Rare:719 | ||||
chr1:66925110-66925530 | Common:14; Rare:728 | ||||
chr1:66929750-66930452 | Common:1; Rare:711 | ||||
chr1:67053590-67053910 | Common:12; Rare:277; Clinvar (pathogenic):1 | ||||
chr1:67053930-67054790 | Common:19; Rare:551 | ||||
chr1:67207352-67207752 | Common:7; Rare:289 | ||||
chr1:67429216-67429911 | Common:5; Rare:385 | ||||
chr1:67429989-67431022 | Common:2; Rare:1392 | ||||
chr1:67684854-67685534 | Common:20; Rare:899 | ||||
chr1:67685803-67686453 | Common:5; Rare:447 | ||||
chr1:67832960-67833290 | Common:1; Rare:76 | ||||
chr1:67833310-67833710 | Common:5; Rare:128 | ||||
chr1:68496410-68497718 | Common:27; Rare:927 | ||||
chr1:70205450-70205790 | Rare:655 | ||||
chr1:70205810-70206427 | Rare:214 |